About this trial

Currently the diagnosis of OA is based on radiographs and clinical findings, which is limited to detecting late-stage disease. There is a pressing, unmet clinical need for robust assessment of early changes in cartilage health. Towards this goal, extensive efforts are ongoing to develop quantitative MRI for cartilage matrix analysis. MR T1ρ and T2 relaxation times have shown to be promising imaging biomarkers for early cartilage degeneration and prediction of disease progression. However, many challenges remain to clinically applying these techniques, including lack of standardized acquisition and quantification methods, and long acquisition times. The study aims to develop novel, fast and reproducible MR T1ρ and T2 relaxation time imaging methods on MR systems from multiple vendors and establish a platform for standardization and cross validation of these measures as a tool for clinical trials using such techniques. Following method validation, patients at risk for osteoarthritis will be tested.

Eligibility criteria

Qualifiers

Age 18-50

Sustain an acute full ACL tear in one knee; the contralateral knee uninjured

Undergo ACL reconstructions and standard rehabilitation

Disqualifiers

Contraindication to MRI such as severe claustrophobia and implanted devices such as neurostimulators, pacemakers, aneurysm clips etc.

Pregnancy.

Contraindication to MRI such as severe claustrophobia and implanted devices such as neurostimulators, pacemakers, aneurysm clips etc.

Pregnancy.

Trial design

Treatments tested in this trial

  • MRI

Treatment groups

88 Participants
are divided into 4 treatment groups

Locations

1
Cleveland Clinic Foundation44195, ClevelandOhio, United States

Sponsors and collaborators

Xiaojuan Li

Lead sponsor

The Cleveland Clinic

Sponsor institution